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Species-specific host factors rather than virus-intrinsic virulence determine primate lentiviral pathogenicity

HIV-1 causes chronic inflammation and AIDS in humans, whereas related simian immunodeficiency viruses (SIVs) replicate efficiently in their natural hosts without causing disease. It is currently unknown to what extent virus-specific properties are responsible for these different clinical outcomes. H...

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Detalles Bibliográficos
Autores principales: Joas, Simone, Parrish, Erica H., Gnanadurai, Clement W., Lump, Edina, Stürzel, Christina M., Parrish, Nicholas F., Learn, Gerald H., Sauermann, Ulrike, Neumann, Berit, Rensing, Kerstin Mätz, Fuchs, Dietmar, Billingsley, James M., Bosinger, Steven E., Silvestri, Guido, Apetrei, Cristian, Huot, Nicolas, Garcia-Tellez, Thalia, Müller-Trutwin, Michaela, Hotter, Dominik, Sauter, Daniel, Stahl-Hennig, Christiane, Hahn, Beatrice H., Kirchhoff, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893559/
https://www.ncbi.nlm.nih.gov/pubmed/29636452
http://dx.doi.org/10.1038/s41467-018-03762-3
Descripción
Sumario:HIV-1 causes chronic inflammation and AIDS in humans, whereas related simian immunodeficiency viruses (SIVs) replicate efficiently in their natural hosts without causing disease. It is currently unknown to what extent virus-specific properties are responsible for these different clinical outcomes. Here, we incorporate two putative HIV-1 virulence determinants, i.e., a Vpu protein that antagonizes tetherin and blocks NF-κB activation and a Nef protein that fails to suppress T cell activation via downmodulation of CD3, into a non-pathogenic SIVagm strain and test their impact on viral replication and pathogenicity in African green monkeys. Despite sustained high-level viremia over more than 4 years, moderately increased immune activation and transcriptional signatures of inflammation, the HIV-1-like SIVagm does not cause immunodeficiency or any other disease. These data indicate that species-specific host factors rather than intrinsic viral virulence factors determine the pathogenicity of primate lentiviruses.